BS ISO 13304-1:2020

The primary purpose of this document is to provide minimum acceptable criteria required to establish a procedure for retrospective dosimetry by electron paramagnetic resonance spectroscopy and to report the results.

The primary purpose of this document is to provide minimum acceptable criteria required to establish a procedure for retrospective dosimetry by electron paramagnetic resonance spectroscopy and to report the results.The second purpose is to facilitate the comparison of measurements related to absorbed dose estimation obtained in different laboratories.This document covers the determination of absorbed dose in the measured material. It does not cover the calculation of dose to organs or to the body. It covers measurements in both biological and inanimate samples, and specifically: based on inanimate environmental materials like glass, plastics, clothing fabrics, saccharides, etc., usually made at X-band microwave frequencies (8GHz to 12GHz); in vitro tooth enamel using concentrated enamel in a sample tube, usually employing X-band frequency, but higher frequencies are also being considered; in vivo tooth dosimetry, currently using L-band (1GHz to 2GHz), but higher frequencies are also being considered; in vitro nail dosimetry using nail clippings measured principally at X-band, but higher frequencies are also being considered; in vivo nail dosimetry with the measurements made at X-band on the intact finger or toe; in vitro measurements of bone, usually employing X-band frequency, but higher frequencies are also being considered. For biological samples, in vitro measurements are carried out in samples after their removal from the person or animal and under laboratory conditions, whereas the measurements in vivo are carried out without sample removal and may take place under field conditions. NOTE The dose referred to in this document is the absorbed dose of ionizing radiation in the measured materials.